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Speech-Language Therapy for Primary Progressive Aphasia

N/A
Recruiting
Led By Stephanie M Grasso, Ph.D
Research Sponsored by University of Texas at Austin
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Meets diagnostic criteria for Primary Progressive Aphasia (PPA; Gorno-Tempini et al., 2011)
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre-phase 1, post-phase1/pre-phase 2 (4.5 weeks from treatment onset), post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatment
Awards & highlights
No Placebo-Only Group

Summary

This trial seeks to study how tailored speech-language interventions help bilingual individuals with PPA. Researchers will evaluate effects of treatment, language use, and brain scans to determine best approach.

Who is the study for?
This trial is for bilingual individuals who speak Spanish and Catalan or Spanish and English, diagnosed with Primary Progressive Aphasia (PPA). Participants must have a certain level of cognitive function as measured by the Mini-Mental State Examination. Those with other central nervous system issues, significant sensory impairments, or prominent non-speech-language impairments cannot join.
What is being tested?
The study tests two speech-language interventions: Video-Implemented Script Training for Aphasia (VISTA) and Lexical Retrieval Training (LRT), tailored for bilingual speakers with PPA. It aims to understand how bilingualism affects treatment response in PPA over time, including follow-ups at 6 and 12 months post-treatment.
What are the potential side effects?
Since this trial involves speech-language therapy rather than medication, traditional side effects are not expected. However, participants may experience fatigue or frustration during the intervention sessions.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have been diagnosed with Primary Progressive Aphasia.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-phase 1, post-phase1/pre-phase 2 (4.5 weeks from treatment onset), post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatment
This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-phase 1, post-phase1/pre-phase 2 (4.5 weeks from treatment onset), post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatment for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Percent correct intelligible words from trained/untrained scripts
Percent correct spoken naming of trained/untrained nouns
Secondary study objectives
Acoustic Features: Articulation Rate
Acoustic Features: Speech-to-pause time
Aphasia Impact Questionnaire (AIQ)
+2 more
Other study objectives
Post-treatment Communication Survey

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Video Implemented Script Training for AphasiaExperimental Treatment2 Interventions
Script training intervention for individuals with nonfluent/agrammatic PPA.
Group II: Lexical Retrieval TrainingExperimental Treatment2 Interventions
Naming intervention for individuals with logopenic or semantic variant PPA.

Find a Location

Who is running the clinical trial?

Hospital Clinic of BarcelonaOTHER
431 Previous Clinical Trials
5,411,162 Total Patients Enrolled
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant PauOTHER
353 Previous Clinical Trials
163,037 Total Patients Enrolled
University of Texas at AustinLead Sponsor
378 Previous Clinical Trials
86,545 Total Patients Enrolled
Stephanie M Grasso, Ph.DPrincipal InvestigatorUniversity of Texas at Austin
Miguel Ángel Santos Santos, MD, PhDPrincipal InvestigatorFundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Media Library

Lexical Retrieval Training (LRT) Clinical Trial Eligibility Overview. Trial Name: NCT05741853 — N/A
Neurodegenerative Disease Research Study Groups: Video Implemented Script Training for Aphasia, Lexical Retrieval Training
Neurodegenerative Disease Clinical Trial 2023: Lexical Retrieval Training (LRT) Highlights & Side Effects. Trial Name: NCT05741853 — N/A
Lexical Retrieval Training (LRT) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05741853 — N/A
~39 spots leftby Nov 2027